FOXD4 (NM 207305) Human Tagged ORF Clone Product Data

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FOXD4 (NM 207305) Human Tagged ORF Clone Product Data

OriGene Technologies, Inc. 9620 Medical Center Drive, Ste 200 Rockville, MD 20850, US Phone: +1-888-267-4436 [email protected] EU: [email protected] CN: [email protected] Product datasheet for RC213792L1 FOXD4 (NM_207305) Human Tagged ORF Clone Product data: Product Type: Expression Plasmids Product Name: FOXD4 (NM_207305) Human Tagged ORF Clone Tag: Myc-DDK Symbol: FOXD4 Synonyms: FKHL9; FOXD4A; FREAC-5; FREAC5 Vector: pLenti-C-Myc-DDK (PS100064) E. coli Selection: Chloramphenicol (34 ug/mL) Cell Selection: None ORF Nucleotide The ORF insert of this clone is exactly the same as(RC213792). Sequence: Restriction Sites: SgfI-MluI Cloning Scheme: ACCN: NM_207305 ORF Size: 1317 bp This product is to be used for laboratory only. Not for diagnostic or therapeutic use. View online » ©2021 OriGene Technologies, Inc., 9620 Medical Center Drive, Ste 200, Rockville, MD 20850, US 1 / 2 FOXD4 (NM_207305) Human Tagged ORF Clone – RC213792L1 OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info OTI Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. RefSeq: NM_207305.2 RefSeq Size: 2204 bp RefSeq ORF: 1320 bp Locus ID: 2298 UniProt ID: Q12950 Protein Families: Transcription Factors MW: 47.3 kDa Gene Summary: This gene encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors. FOX transcription factors play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. Mutations in this gene are associated with a complex phenotype consisting of dilated cardiomyopathy, obsessive-compulsive disorders, and suicidality. [provided by RefSeq, Mar 2012] Product images: Double digestion of RC213792L1 using SgfI and MluI This product is to be used for laboratory only. Not for diagnostic or therapeutic use. ©2021 OriGene Technologies, Inc., 9620 Medical Center Drive, Ste 200, Rockville, MD 20850, US 2 / 2.

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